Clinical trial designs for testing of products for dentine hypersensitivity--a review.

D G Gillam
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Abstract

Dentine hypersensitivity (DH) is a perplexing clinical entity. There is no doubt that patients self-report discomfort arising from various stimuli, but the highly subjective nature of the condition makes it extremely difficult to evaluate DH objectively. This is particularly true when evaluating the efficacy of desensitizing agents in the clinical trial setting. This paper attempts to provide an overview on clinical trial management to evaluate both in-office and over-the-counter (OTC) desensitizing agents. The importance of correct clinical trial design (type, allocation, blinding) with emphasis on patient selection, sample size, statistical power, duration, choice of positive/negative controls, treatment outcomes, and data collection, will be discussed.

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牙本质过敏产品试验的临床试验设计综述。
牙本质过敏症(DH)是一个令人困惑的临床问题。毫无疑问,患者自我报告各种刺激引起的不适,但这种情况的高度主观性使得客观评估DH极其困难。在临床试验中评估脱敏剂的疗效时尤其如此。本文试图提供临床试验管理的概述,以评估在办公室和非处方(OTC)脱敏剂。将讨论正确临床试验设计(类型、分配、盲法)的重要性,重点是患者选择、样本量、统计效力、持续时间、阳性/阴性对照的选择、治疗结果和数据收集。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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